Disease #00458 (DMBCYP2D6 (metabolism, drug, poor/rapid), OMIM:608902)
Official abbreviation |
DMBCYP2D6 |
Name |
metabolism, drug, poor/rapid |
OMIM ID |
608902 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
5 |
Phenotype entries for this disease |
5 |
Associated with 1 gene |
CYP2D6 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-07-14 13:05:48 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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